OMOP Concept 4134552
Hereditary motor and sensory neuropathy
StandardConditionSNOMED398100001Disorder
Maps from
25
Descendants
108
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
25 source codes normalize to Hereditary motor and sensory neuropathy via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Hereditary motor and sensory neuropathy across source vocabularies.
- CMT - Charcot-Marie-Tooth disease
- enfermedad de Charcot Marie Tooth
- enfermedad de CMT (Charcot Marie Tooth)
- Hereditary motor and sensory neuropathy (disorder)
- Hereditary sensorimotor neuropathy
- Hereditary sensory and motor neuropathy
- Hereditary sensory-motor neuropathy
- HMSN - hereditary motor and sensory neuropathy
- HSMN - hereditary sensory and motor neuropathy
- neuropatía sensitiva y motriz hereditaria
- neuropatía sensitiva y motriz hereditaria (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(108)Included automatically when you query with descendants.
- 1Andermann syndrome
- 1Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
- 1Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
- 1Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
- 1Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
- 1Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
- 1Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
- 1Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
- 1Autosomal dominant slowed nerve conduction velocity
- 1Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
- 1Autosomal recessive intermediate Charcot-Marie-Tooth disease type A
- 1Autosomal recessive intermediate Charcot-Marie-Tooth disease type B
- 1Autosomal recessive intermediate Charcot-Marie-Tooth disease type C
- 1Autosomal recessive intermediate Charcot-Marie-Tooth disease type D
- 1Autosomal recessive lethal neonatal axonal sensorimotor polyneuropathy
- 1Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome
- 1Charcot-Marie-Tooth disease type 4
- 1Charcot-Marie-Tooth disease, type II
- 1Charcot-Marie-Tooth Neuropathy Type 4
- 1Congenital axonal neuropathy with encephalopathy
- 1Déjérine-Sottas disease
- 1Digital extensor muscle aplasia with polyneuropathy
- 1Hereditary motor and sensory neuropathy Okinawa type
- 1Hereditary motor and sensory neuropathy type 5
- 1Hereditary motor and sensory neuropathy with acrodystrophy
- 1Hereditary motor and sensory neuropathy with optic atrophy
- 1Hereditary motor and sensory neuropathy with retinitis pigmentosa
- 1Hereditary sensorimotor neuropathy with hyperelastic skin
- 1Hereditary sensory-motor neuropathy, type I
- 1Hereditary sensory neuropathy
- 1Hereditary thermosensitive neuropathy
- 1HSMN IV
- 1Infantile-onset axonal motor and sensory neuropathy, optic atrophy, neurodegenerative syndrome
- 1Microcephalus, complex motor and sensory axonal neuropathy syndrome
- 1Palmoplantar keratoderma, hereditary motor and sensory neuropathy syndrome
- 1PMP22-RAI1 contiguous gene duplication syndrome
- 1Roussy-Lévy syndrome
- 1Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
- 1X-linked hereditary motor and sensory neuropathy
- 2Ataxia co-occurrent and due to phytanic acid storage disease
- 2Autosomal dominant Charcot-Marie-Tooth disease type 2
- 2Autosomal recessive Charcot-Marie-Tooth disease type 2
- 2Cataract, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, skeletal dysplasia syndrome
- 2Charcot-Marie-Tooth disease type 2P
- 2Charcot-Marie-Tooth disease type 4A
- 2Charcot-Marie-Tooth disease type 4B1
- 2Charcot-Marie-Tooth disease type 4B2
- 2Charcot-Marie-Tooth disease type 4B3
- 2Charcot-Marie-Tooth disease type 4C
- 2Charcot-Marie-Tooth disease type 4D
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